Literature DB >> 23608144

Sequence and structure-specific elements of HERG mRNA determine channel synthesis and trafficking efficiency.

Jakub Sroubek1, Yamini Krishnan, Thomas V McDonald.   

Abstract

Human ether-á-gogo-related gene (HERG) encodes a potassium channel that is highly susceptible to deleterious mutations resulting in susceptibility to fatal cardiac arrhythmias. Most mutations adversely affect HERG channel assembly and trafficking. Why the channel is so vulnerable to missense mutations is not well understood. Since nothing is known of how mRNA structural elements factor in channel processing, we synthesized a codon-modified HERG cDNA (HERG-CM) where the codons were synonymously changed to reduce GC content, secondary structure, and rare codon usage. HERG-CM produced typical IKr-like currents; however, channel synthesis and processing were markedly different. Translation efficiency was reduced for HERG-CM, as determined by heterologous expression, in vitro translation, and polysomal profiling. Trafficking efficiency to the cell surface was greatly enhanced, as assayed by immunofluorescence, subcellular fractionation, and surface labeling. Chimeras of HERG-NT/CM indicated that trafficking efficiency was largely dependent on 5' sequences, while translation efficiency involved multiple areas. These results suggest that HERG translation and trafficking rates are independently governed by noncoding information in various regions of the mRNA molecule. Noncoding information embedded within the mRNA may play a role in the pathogenesis of hereditary arrhythmia syndromes and could provide an avenue for targeted therapeutics.

Entities:  

Keywords:  KCNH2; LQTS; SNP; codon-usage; protein translation

Mesh:

Substances:

Year:  2013        PMID: 23608144      PMCID: PMC3714577          DOI: 10.1096/fj.12-227009

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  65 in total

1.  Secondary structure of the ribosome binding site determines translational efficiency: a quantitative analysis.

Authors:  M H de Smit; J van Duin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

2.  Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.

Authors:  Julien Barc; François Briec; Sébastien Schmitt; Florence Kyndt; Martine Le Cunff; Estelle Baron; Claude Vieyres; Frédéric Sacher; Richard Redon; Cédric Le Caignec; Hervé Le Marec; Vincent Probst; Jean-Jacques Schott
Journal:  J Am Coll Cardiol       Date:  2011-01-04       Impact factor: 24.094

3.  mRNA helicase activity of the ribosome.

Authors:  Seyedtaghi Takyar; Robyn P Hickerson; Harry F Noller
Journal:  Cell       Date:  2005-01-14       Impact factor: 41.582

Review 4.  Understanding the contribution of synonymous mutations to human disease.

Authors:  Zuben E Sauna; Chava Kimchi-Sarfaty
Journal:  Nat Rev Genet       Date:  2011-08-31       Impact factor: 53.242

5.  A family of potassium channel genes related to eag in Drosophila and mammals.

Authors:  J W Warmke; B Ganetzky
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-12       Impact factor: 11.205

6.  A minK-HERG complex regulates the cardiac potassium current I(Kr).

Authors:  T V McDonald; Z Yu; Z Ming; E Palma; M B Meyers; K W Wang; S A Goldstein; G I Fishman
Journal:  Nature       Date:  1997-07-17       Impact factor: 49.962

7.  Translation is a non-uniform process. Effect of tRNA availability on the rate of elongation of nascent polypeptide chains.

Authors:  S Varenne; J Buc; R Lloubes; C Lazdunski
Journal:  J Mol Biol       Date:  1984-12-15       Impact factor: 5.469

Review 8.  Codon usage patterns in Escherichia coli, Bacillus subtilis, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Drosophila melanogaster and Homo sapiens; a review of the considerable within-species diversity.

Authors:  P M Sharp; E Cowe; D G Higgins; D C Shields; K H Wolfe; F Wright
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

9.  HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects.

Authors:  Z Zhou; Q Gong; M L Epstein; C T January
Journal:  J Biol Chem       Date:  1998-08-14       Impact factor: 5.157

10.  A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.

Authors:  M C Sanguinetti; C Jiang; M E Curran; M T Keating
Journal:  Cell       Date:  1995-04-21       Impact factor: 41.582

View more
  4 in total

1.  Ion channels under the sun.

Authors:  Geoffrey W Abbott; Geoffrey S Pitt
Journal:  FASEB J       Date:  2014-05       Impact factor: 5.191

2.  Synonymous nucleotide modification of the KCNH2 gene affects both mRNA characteristics and translation of the encoded hERG ion channel.

Authors:  Alexander C Bertalovitz; Marika L Osterbur Badhey; Thomas V McDonald
Journal:  J Biol Chem       Date:  2018-06-15       Impact factor: 5.157

3.  A synonymous codon change alters the drug sensitivity of ΔF508 cystic fibrosis transmembrane conductance regulator.

Authors:  Vedrana Bali; Ahmed Lazrak; Purushotham Guroji; Lianwu Fu; Sadis Matalon; Zsuzsanna Bebok
Journal:  FASEB J       Date:  2015-09-03       Impact factor: 5.191

4.  A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity.

Authors:  Barbara Oliveira-Mendes; Sylvain Feliciangeli; Mélissa Ménard; Frank Chatelain; Malak Alameh; Jérôme Montnach; Sébastien Nicolas; Béatrice Ollivier; Julien Barc; Isabelle Baró; Jean-Jacques Schott; Vincent Probst; Florence Kyndt; Isabelle Denjoy; Florian Lesage; Gildas Loussouarn; Michel De Waard
Journal:  Clin Transl Med       Date:  2021-11
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.